Hello, and welcome, everyone, joining today's Nouvelle's 4th Quarter 2025 Earnings Conference Call. At this time, all participants are in a listen-only mode. Later, you will have the opportunity to ask questions during the question-and-answer session. To register to ask a question at any time, please press star 1 on your telephone keypad. Please note this call has been recorded. We are standing by if you should need any assistance. It is now my pleasure to turn the meeting over to Leah McMullen, Director of Communications. Please go ahead.

Thank you, Operator. Thank you all for joining today's conference call to discuss New Ellis' corporate developments and financial results for the fourth quarter and full year as of December 31, 2025. In addition to myself, with us today are John Erb, New Ellis' Chairman of the Board and CEO, and our newly appointed CFO, Carissa Schultz. At 8 a.m. Eastern Time today, New Ellis released financial results for the fourth quarter and full year 2025. If you have not received New Ellis' earnings, please visit the Investor page on the company's website. During the conference call, the company will be making forward-looking statements. All forward-looking statements made during today's call will be protected under the Private Securities Litigation Reform Act of 1995. Any statements that relate to expectations or predictions of future events and market trends as well as our estimated results or performance are forward-looking statements. All forward-looking statements are based upon our current estimates and various assumptions. These statements involve material risks and uncertainties that could cause actual results or events to materially differ from those anticipated or implied by these forward-looking statements. All forward-looking statements are based upon current available information, and the company assumes no obligation to update these statements. Accordingly, you should not place undue reliance on these statements. Please refer to the cautionary statements and discussion of risk in the company's filings with the Securities and Exchange Commission, including the latest 10K. With that, I would now like to turn the call over to John.

Thank you, Leah, and good morning, everyone. I would like to begin by stepping back from the quarter and reflecting on the year as a whole. 2025 was not a continuation year for New Ellis. It was a year of structural change and deliberate repositioning. While full-year revenue declined 5% compared to 2024, the defining characteristic of 2025 was not top-line variability. It was the strengthening of the company's operating foundation and the clarification of our long-term strategy. Throughout the year, we made intentional decisions to simplify the business, improve operational discipline, and concentrate resources in areas where clinical adoption and economic value are most aligned. A central initiative was the transition of manufacturing to KDI precision manufacturing. This was a significant operational undertaking requiring coordination across supply chain, quality systems, and production leadership. The objective was not short-term cost reduction. It was long-term reliability, scalable manufacturing alignment, and improved structural margin performance. As we move forward, this transition enhances operational predictability and strengthens our supply chain foundation. We also evaluated and refined our international commercial strategy. Portions of that business generated inconsistent returns and required disproportionate resources. During the year, we reduced exposure in certain markets and redirected focus towards geographies where clinical demand and commercial conversion are more predictable. That decision reflects discipline and prioritization. Over the course of the year, we also maintained access to capital through financing transitions that supported operational continuity during a period of transition. We ended the year with approximately $1.2 million in cash and no outstanding debt. Liquidity management and disciplined capital allocation remain central priorities as we execute our strategy. Beyond operational and financial refinements, 2025 marked a critical clarification of strategic positioning. Historically, Nuelis has been described as a fluid management company. Over the course of the year, we sharpened our focus around the cardiorenal continuum. Our technology serves patients whose cardiac and renal conditions are tightly interrelated and where precision volume management directly influences outcomes across both organ systems. This alignment reflects where we see the strongest clinical traction and the most durable long-term opportunity. Growth in heart failure and pediatrics reinforces that our value proposition is most compelling within complex cardiorenal populations. Within this strategy, our pediatric program represents a meaningful extension of our platform. During the year, we expanded intellectual property supporting our pediatric device development and were the beneficiary of a National Institute of Health grant to advance this program. The combination of strengthened IP and non-dilutive NIH funding provides external validation of the clinical importance of this work and reinforces the long-term defensibility of our innovation within the cardiorenal continuum. Turning to the fourth quarter, revenue was $2.4 million, an increase of 4% compared to the prior year quarter, and 9% sequentially. U.S. console sales increased 208%, reflecting stronger activity within targeted accounts. Gross margin expanded to 68.2% in the quarter, compared to 58.4% in the prior year period. Full-year operating expenses were $400,000 lower than the prior year, reflecting tighter expense management, improved forecasting discipline, and more selective commercial deployment. These results reinforce a core operating principle. Where clinical adoption is established, utilization expands. Our strategy is not broad-based expansion across all possible customer opportunities. It is discipline, concentration, and accounts and patient populations where clinical pull and economic value are demonstrable. Taken together, 2025 was a year of operational strengthening, portfolio alignment, discipline, capital management, and strategic clarity. The organization enters 2026 more focused, more disciplined, and structurally stronger than it was a year ago. As we begin 2026, we have further strengthened our financial leadership. Earlier this year, we welcomed Carissa Schultz as Chief Financial Officer. Carissa brings deep experience in medical technology, finance, and operational leadership. Her focus on forecasting precision, capital allocation discipline, and financial transparency supports the operating model we have refined over the past year. With that, I will turn the call over to Chris for a detailed review of our financial results.

Thank you, John, and good morning. I will begin with fourth quarter performance before turning to full year results in our balance sheet position. Revenue for the fourth quarter of 2025 was $2.4 million, representing a 4% increase compared to the prior year quarter and a 9% increase sequentially. The year-over-year improvement was driven by a 208% increase in U.S. consult sales, with eight units sold compared to three in the prior year period, and an 11% circuit average selling price increase. International sales increased 59% year-over-year, largely as a result of last-time buys from distributors whose territories we were exiting. These gains were partially offset by a 24 percent decline in critical care revenue. Sequentially, revenue growth was driven primarily by increased catheter utilization, partially offset by lower console sales compared to the third quarter. Gross margin for the fourth quarter was 68.2 percent, an improvement of 9.9 percentage points compared to the prior year quarter. Operating expenses for the quarter were $4.1 million, representing a $0.4 million increase compared to the prior year quarter. The year-over-year increase reflects higher professional services, recruiting activity, and targeted development initiatives. Operating loss for the fourth quarter was $2.4 million, flat with the prior year quarter. Net loss attributable to common shareholders for the quarter was $2.4 million. Turning to full-year results, revenue for 2025 was $8.3 million, a 5% decrease compared to the prior year. The year-over-year decline reflects lower consumables utilization, lower U.S. console average selling prices, reduced international contributions following strategic rationalization, and prior year C-star sales prior to that agreement termination. Heart failure of pediatrics grew 8% and 14% year-over-year, respectively, partially offset by a 19% decline in critical care. Full-year gross margin was 62%, 3% lower than the prior year. Operating expenses for the full year were $16.2 million, slightly lower than the prior year, reflecting improved expense discipline and forecasting rigor. Net loss attributable to common shareholders for the full year was $17.5 million, which includes a $6.4 million non-cash warrant valuation expense and approximately $0.3 million in executive severance expense. From a liquidity standpoint, full-year cash utilization was approximately $10.9 million. Weeks end of the year, we ended the year with approximately $1.2 million in cash and no outstanding debt. During 2025, we raised approximately $7 million in net proceeds through financing activities, supporting operations during a period of structural transition. As we move into 2026, our financial priorities remain focused on gross margin consistency, disciplined expense management, enhanced visibility into commercial conversion, and prudent capital deployment. This concludes our prepared remarks. Operator, we would now like to open the call to questions.

And if you would like to ask a question, please press star 1 on your keypad. To leave the queue at any time, press star 2. Once again, that is star and 1 to ask a question. And we will pause for just a moment to allow everyone a chance to join the queue. And once again, that is star and 1 if you would like to join the queue. We are showing one question comes from the line of Anthony Vendetti with Maxim Group. Please go ahead. Your line is open.

Thank you. So I wanted to, John, just talk about, you know, you said you had some operational changes this year and a refocus of the business. Can you talk a little bit about, you know, where the sales force and where your main focus is now versus where it was maybe a couple of years ago. And then also, the second part of the question is going to be on the REND Tech, if I'm pronouncing it correct, the acquisition, how those products are going to be incorporated into your current product portfolio.

Sure, Anthony. Well, let me start off and say that in 2025, we reinforced our direct sales team. We had declined the beginning of the year by several account territories, and we brought some folks on board, both account managers and clinical specialists, to bring us back up to the budgeted amount. which really we saw that impact in the second half of the year, really beginning to see much greater growth in the beginning of 2026. You know, at the beginning of the year, this year, we were recovering from a product recall and from some quality issues that we really needed to redirect the business. And that was the primary reason we ended up going to contract manufacturing with KDI precision manufacturing. That's really brought a stableness to our supply and product quality that we're very pleased with. We also look hard at expenses, looking at our cash burn and how could we reduce it internationally, particularly in the European Union. We have lost money continually year after year. we made the decision that we would exit the EU and basically successfully pulled out of that and reduced our cash burn. We also looked hard at an expensive clinical trial that was in place with the reverse HF clinical trial. It was budgeted to spend an additional $3 million dollars to complete the trial, take a couple of years, and the benefit of a very successful trial was still going to be two or three years down the road. So again, looking at cash management, we made the decision to terminate that trial. We are actively now working with the principal investigators with the data that was completed to put together a publication with some positive results. So a lot of activity around refocusing the business. You know, the NIH grant that we received for pediatrics, development of the renal replacement therapy device is very positive for us and we continue to grow in the pediatrics area. So I'd say that a bit of a refocus, not so much away from heart failure, but in addition to heart failure, really focusing on the pediatric nephrologist and the benefit that the Aquadex product was bringing to the pediatric marketplace. Let's see, what else? I think that covered your main question. The second part of your question regarding Erendia Tech, the value there is in critical care. You know, as we remove fluid after a patient has come off of the heart-lung machine very gently and very carefully, which is what the heart needs, what the kidneys need, you know, after extubation from the heart-lung machine. They also measure all the fluid off, and renal output or urine output is another critical measure. What Rendia Tech has is a technology basically that helps measure that renal or urine output in the ICU. What's exciting about that product is the opportunity that we're already working on is to enhance the capability of not just measuring flow and measuring quantity, but also measuring the analytes or electrolytes that are in the urine. That is a key biomarker for kidney health, acute kidney injury. About 60% of patients in critical care that come off of the heart-lung machine do experience acute kidney injury. Rather than that urine being sent to the lab and waiting for lab results to come back to look at the potassium, sodium, oxygen level in the urine, they can get this bedside. So that's, that was really the primary reason we were interested in the Rindia Tech acquisition is that very differentiated capability that it will bring to the ICU.

Okay, John, that's helpful. Maybe since it looked like fourth quarter sales was driven more by utilization within existing accounts versus new accounts. So Rindia Tech is the focus going to be to try to get more utilization out of the current accounts as we begin this year and try to get RendiaTech into all those accounts? And then where is your sales force or territory manager number currently? And is that expected to be constant for this year, or do you expect to add as you move through the year?

Thanks. Sure. Well, let me start with the second part of that question, and that right now, our total sales team is 24 individuals between account managers and clinical specialists, and that really brings it up to what was budgeted for headcount in 2025, and I anticipate keeping it at that number through 2026. We have a lot of opportunity in existing accounts. And, you know, this is the first part of your question. We will focus on improved or increased utilization. The sales team is primarily focused on critical care. We see critical care, ICU, the cardiorenal issue in these patients that have gone through cardiac surgery has really a big opportunity for the company, so that's a primary focus. Of course, we will continue to support our heart failure customers and patients and working closely in nephrology in the pediatric area as a product's used, but I would say that the majority of the focus is to grow the critical care business in existing accounts. A lot of these accounts are already heart failure accounts that we are expanding into critical care. And we see the Rindia Tech acquisition as an opportunity to enhance utilization within those accounts.

Okay. Thanks so much. That's very helpful. I'll jump back in the queue.

Thank you. And once again, if you would like to ask a question, please press star 1 on your keypad now.

We'll pause for another moment. And once more, that is star and 1 if you would like to join the queue. Thank you.

And at this time, there are no further questions in queue. I will now turn the meeting back to management for closing remarks.

Thank you. 2025 marked a necessary inflection point for the company. We made decisive adjustments to strengthen the operating model and clarify our strategic focus. As we enter 2026, we are doing so with renewed momentum, including the execution of our agreement to acquire Rendia Tech and the planned expansion of our portfolio, the appointment of Ms. Schultz as our Chief Financial Officer, and additional capital to support operations. Entering this next phase, we are more disciplined, more deliberate, and aligned around the cardiorenal opportunity that will define our next phase of growth. The structural work completed in 2025 positions us to shift from refinement to execution in 2026. Our objective in 2026 is to translate strategic clarity into more predictable commercial performance. We will continue executing with discipline, concentrating resources in cardiorenal populations where clinical adoption and utilization are strongest, and driving deeper penetration within active accounts. We are actively integrating our recent acquisition of Rundi Tech and plan to relaunch the Clarity product mid-year. We also continue progressing development of Vivian, our novel pediatric solution supported by the NIH grant funding. We will maintain financial rigor, strengthen margin consistency, and prioritize capital efficiency as we scale. We appreciate the continued support of our shareholders, the drive and focus of our team, and look forward to updating you on progress throughout the year. Thank you, and goodbye.

Thank you. This brings us to the end of today's meeting. We appreciate your time and participation. You may now disconnect.